Northwestern scientists have developed a new nanostructure that supercharges CRISPR’s ability to safely and efficiently enter cells, potentially unlocking its full power to treat genetic diseases. By ...

Dublin, Jan. 13, 2025 (GLOBE NEWSWIRE) -- The "CRISPR-based Gene Editing Market by Product & Service, by Application, by End-User, and By Region" report has been added to ResearchAndMarkets.com's ...

The global CRISPR-based gene editing market size is projected to grow from USD 4.46 billion in 2025 to over USD 13.39 billion by 2034, expanding at a CAGR of 13%. Growth is fueled by advancements in ...

A study, published in the journal Frontiers in Genome Editing, outlines a method for editing single plant cells from sterile ...

CRISPR gene-edited cell therapy improves quality of life in patients with transfusion-dependent beta-thalassemia, research suggests.

Horses with genomic edits to make them run faster have been banned from polo, but a zoo of CRISPR-edited animals is gaining ...

Multisystemic smooth muscle dysfunction syndrome (MSMDS) is a rare condition associated with stroke, aortic dissection (tearing) and death in ...

Patients are about to be enrolled in the first study to test a gene-editing technique known as CRISPR inside the body to try to cure an inherited form of blindness. People with the disease have normal ...

Multisystemic smooth muscle dysfunction syndrome (MSMDS) is a rare condition associated with stroke, aortic dissection ...

Researchers engineered and screened dozens of base editors to precisely target a single mutation without editing other portions of the DNA.

It may sound like something from a fiction movie, and just over a decade ago it probably was, but in that time, scientists have discovered a ground-breaking genetic engineering tool called CRISPR-Cas9 ...

Investigators have used base editing to create a treatment for multisystemic smooth muscle dysfunction syndrome, which has ...